| Literature DB >> 27932698 |
Patrick R Visperas1,2, Christopher G Wilson3, Jonathan A Winger1,4, Qingrong Yan1,5, Kevin Lin1, Michelle R Arkin3, Arthur Weiss6, John Kuriyan1,7.
Abstract
ZAP-70 is a critical molecule in the transduction of T cell antigen receptor signaling and the activation of T cells. Upon activation of the T cell antigen receptor, ZAP-70 is recruited to the intracellular ζ-chains of the T cell receptor, where ZAP-70 is activated and colocalized with its substrates. Inhibitors of ZAP-70 could potentially function as treatments for autoimmune diseases or organ transplantation. In this work, we present the design, optimization, and implementation of a screen for inhibitors that would disrupt the interaction between ZAP-70 and the T cell antigen receptor. The screen is based on a fluorescence polarization assay for peptide binding to ZAP-70.Entities:
Keywords: T cell; ZAP-70; covalent inhibitor; fluorescence polarization (FP); kinase; time-resolved fluorescence resonance energy transfer (TR-FRET)
Mesh:
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Year: 2016 PMID: 27932698 PMCID: PMC5491343 DOI: 10.1177/1087057116681407
Source DB: PubMed Journal: SLAS Discov ISSN: 2472-5552 Impact factor: 3.341